Methicillin-resistant Staphylococcus aureus

被引:0
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作者
Andie S. Lee
Hermínia de Lencastre
Javier Garau
Jan Kluytmans
Surbhi Malhotra-Kumar
Andreas Peschel
Stephan Harbarth
机构
[1] Royal Prince Alfred Hospital,Departments of Infectious Diseases and Microbiology
[2] Faculty of Medicine,Department of Medicine
[3] University of Sydney,Department of Infection Control
[4] Laboratory of Microbiology and Infectious Diseases,Infection Biology Department
[5] The Rockefeller University,undefined
[6] Laboratory of Molecular Genetics,undefined
[7] Instituto de Tecnologia Química e Biológica António Xavier,undefined
[8] Universidade Nova de Lisboa,undefined
[9] Hospital Universitari Mutua de Terrassa,undefined
[10] Amphia Hospital,undefined
[11] Julius Center for Health Sciences and Primary Care,undefined
[12] University Medical Center Utrecht,undefined
[13] Utrecht University,undefined
[14] Laboratory of Medical Microbiology,undefined
[15] Vaccine and Infectious Disease Institute,undefined
[16] Universiteit Antwerpen,undefined
[17] Interfaculty Institute of Microbiology and Infection Medicine,undefined
[18] University of Tübingen,undefined
[19] German Center for Infection Research,undefined
[20] Partner Site Tübingen,undefined
[21] Infection Control Programme,undefined
[22] University of Geneva Hospitals and Faculty of Medicine,undefined
[23] WHO Collaborating Center,undefined
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摘要
Since the 1960s, methicillin-resistant Staphylococcus aureus (MRSA) has emerged, disseminated globally and become a leading cause of bacterial infections in both health-care and community settings. However, there is marked geographical variation in MRSA burden owing to several factors, including differences in local infection control practices and pathogen-specific characteristics of the circulating clones. Different MRSA clones have resulted from the independent acquisition of staphylococcal cassette chromosome mec (SCCmec), which contains genes encoding proteins that render the bacterium resistant to most β-lactam antibiotics (such as methicillin), by several S. aureus clones. The success of MRSA is a consequence of the extensive arsenal of virulence factors produced by S. aureus combined with β-lactam resistance and, for most clones, resistance to other antibiotic classes. Clinical manifestations of MRSA range from asymptomatic colonization of the nasal mucosa to mild skin and soft tissue infections to fulminant invasive disease with high mortality. Although treatment options for MRSA are limited, several new antimicrobials are under development. An understanding of colonization dynamics, routes of transmission, risk factors for progression to infection and conditions that promote the emergence of resistance will enable optimization of strategies to effectively control MRSA. Vaccine candidates are also under development and could become an effective prevention measure.
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